# Spatz FGIA, Inc – FDA Inspection, Aug 9, 2019

Source: https://www.keypedia.com/records/fda_inspections/spatz-fgia-inc/b9213149-9d74-4dcf-92e4-fe39c56e5353
Source feed: FDA_Inspections

> FDA inspection 1099803 of Spatz FGIA, Inc, August 09, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1099803
- Company Name: Spatz FGIA, Inc
- Inspection Date: 2019-08-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1194697 - 2022-12-15
- FDA Inspection 1107557 - 2019-09-25

## Related Officers

- [Investigator](https://www.keypedia.com/people/richard-w-berning/4637e321-8803-4fcf-911f-bbc810c3487d)

Company: https://www.keypedia.com/companies/spatz-fgia-inc/6969606d-c6f8-4971-8c44-2027dc286d4d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7